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dc.contributor.authorFang, Zeguo
dc.contributor.authorCordes, David B.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorO'Hagan, David
dc.date.accessioned2020-08-08T23:37:13Z
dc.date.available2020-08-08T23:37:13Z
dc.date.issued2019-09-14
dc.identifier260562094
dc.identifier12428270-33e7-47e2-ba32-9fade2c284b1
dc.identifier85071618639
dc.identifier000483700100006
dc.identifier.citationFang , Z , Cordes , D B , Slawin , A M Z & O'Hagan , D 2019 , ' Fluorine containing cyclopropanes : synthesis of aryl substituted all- cis 1,2,3-trifluorocylopropanes, a facially polar motif ' , Chemical Communications , vol. 55 , no. 71 , pp. 10539-10542 . https://doi.org/10.1039/C9CC05749Hen
dc.identifier.issn1359-7345
dc.identifier.otherBibtex: urn:b696f326f8c1c6926412b893cb0f5902
dc.identifier.otherORCID: /0000-0002-9527-6418/work/60630651
dc.identifier.otherORCID: /0000-0002-5366-9168/work/60630656
dc.identifier.otherORCID: /0000-0002-0510-5552/work/68281251
dc.identifier.urihttps://hdl.handle.net/10023/20430
dc.descriptionWe thank the EPSRC for financial support (GR: EP/R013799/1) and we are grateful to the Chinese Scholarship Council (CSC) for Ph.D Studentship support (ZF).en
dc.description.abstractThe synthesis of substituted all-cis-1,2,3-trifluorocylopropanes are described for the first time. The three fluorines located on each of the cyclopropyl carbons with a stereochemistry where they are all on the same face of the cyclopropane, imparts a significant polarity to the molecule, and the inherent conformational rigidity and lowering of Log P makes this motif attractive for exploration as a substituent for pharmaceuticals and agrochemicals research.
dc.format.extent1123709
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleFluorine containing cyclopropanes : synthesis of aryl substituted all-cis 1,2,3-trifluorocylopropanes, a facially polar motifen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.1039/C9CC05749H
dc.description.statusPeer revieweden
dc.date.embargoedUntil2020-08-09
dc.identifier.grantnumberEP/R013799/1en


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